ZipRecruiter

Log In

1

Clinical Research Associate Trainee Jobs in Raleigh, NC

Veranex

Sr Clinical Research Associate

Raleigh, NC · On-site

$98K - $140K/yr

Veranex has an exciting opportunity to join our team as a Senior Clinical Research Associate to support our Clinical Operations team. The Sr. CRA will participate in the planning, development, and ...

Icon plc

Senior Clinical Research Associate

Cary, NC · Remote

Extensive experience as a Clinical Research Associate, with a strong understanding of clinical trial processes and regulatory requirements. * Proven ability to manage multiple sites and projects ...

IQVIA

Sr. Clinical Research Associate, IQVIA

Durham, NC

$87K - $169K/yr

IQVIA is hiring Senior Clinical Research Associate 1 with experience in either oncology, cardiovascular, renal, metabolic, CNS, Obesity (GLP-1), diabetes, GI, MASH/NASH, dermatology, or respiratory:

IQVIA

Sr. Clinical Research Associate, IQVIA

Durham, NC

$87K - $169K/yr

IQVIA is hiring Senior Clinical Research Associate 1 with experience in either oncology, cardiovascular, renal, metabolic, CNS, Obesity (GLP-1), diabetes, GI, MASH/NASH, dermatology, or respiratory:

IQVIA

Clinical Research Associate 2, IQVIA

Durham, NC

$71K - $189K/yr

IQVIA is hiring a Clinical Research Associate 2 with on-site monitoring experience in IM/GI, MASH/NASH, dermatology and/or asthma/respiratory clinical trials. Women's Health experience is a plus! Job ...

IQVIA

Clinical Research Associate 2, IQVIA

Durham, NC

$71K - $189K/yr

IQVIA is hiring a Clinical Research Associate 2 with on-site monitoring experience in IM/GI, MASH/NASH, dermatology and/or asthma/respiratory clinical trials. Women's Health experience is a plus! Job ...

IQVIA, Inc.

Clinical Research Associate 2, IQVIA

Durham, NC · On-site

$71K - $189K/yr

IQVIA is hiring a Clinical Research Associate 2 with on-site monitoring experience in IM/GI, MASH/NASH, dermatology and/or asthma/respiratory clinical trials. Women's Health experience is a plus! Job ...

IQVIA

Clinical Research Associate

Durham, NC · On-site

$87K - $182K/yr

Req Good knowledge of, and skill in applying, applicable clinical research regulatory requirements. i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.

IQVIA

Clinical Research Associate

Durham, NC · On-site

$71K - $189K/yr

Req Good knowledge of, and skill in applying, applicable clinical research regulatory requirements (i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines)

next page

Showing results 1-20

All JobsClinical Research Associate JobsClinical Research Associate Trainee JobsClinical Research Associate Trainee Jobs in Raleigh, NC

Clinical Research Associate Trainee information

See Raleigh, NC salary details

$12

$30

$53

How much do clinical research associate trainee jobs pay per hour?

As of Aug 9, 2026, the average hourly pay for clinical research associate trainee in Raleigh, NC is $30.66, according to ZipRecruiter salary data. Most workers in this role earn between $20.58 and $40.43 per hour, depending on experience, location, and employer.

What types of projects and studies can a clinical research associate trainee expect to work on during their first year?

As a Clinical Research Associate Trainee, you will typically be involved in assisting with a variety of clinical trials, ranging from early-phase (Phase I/II) to later-phase (Phase III/IV) studies. Your responsibilities may include site monitoring, verifying that clinical data is accurately recorded, and ensuring compliance with regulatory guidelines. You'll often work closely with senior CRAs, study coordinators, and investigators, allowing you to gain hands-on experience with protocols and Good Clinical Practice (GCP) standards. This exposure prepares you for more independent monitoring roles as you progress in your career.

What are the key skills and qualifications needed to thrive as a clinical research associate trainee, and why are they important?

To thrive as a Clinical Research Associate Trainee, you need a solid background in life sciences or a related field, strong organizational skills, and keen attention to detail. Familiarity with clinical trial management systems (CTMS), Good Clinical Practice (GCP) guidelines, and relevant certifications such as GCP training are typically required. Excellent communication, problem-solving abilities, and adaptability are important soft skills for building relationships with site staff and ensuring protocol compliance. These skills and qualities are vital for maintaining data integrity, patient safety, and regulatory adherence throughout the clinical trial process.

What is the difference between Clinical Research Associate Trainee vs Clinical Research Associate?

AspectClinical Research Associate TraineeClinical Research Associate
Required CredentialsOften entry-level, may require a bachelor's degree in life sciences or related fieldRequires relevant experience, often a bachelor's degree and certification
Work EnvironmentTraining programs, supervised settings, clinical trial sitesIndependent monitoring at clinical sites, data review, regulatory compliance
Employer & Industry UsagePharmaceutical companies, CROs, biotech firms during training phaseEstablished professionals working in similar organizations

The Clinical Research Associate Trainee is an entry-level position focused on learning and training, often requiring minimal experience. In contrast, a Clinical Research Associate is a more experienced role responsible for monitoring clinical trials independently. The trainee role serves as a stepping stone toward becoming a full Clinical Research Associate.

What is a clinical research associate trainee?

Clinical Research Associate (CRA) Trainees are entry-level professionals who assist in the monitoring, coordination, and administration of clinical trials. They work under the supervision of experienced CRAs to ensure that clinical research studies comply with regulatory requirements, protocols, and ethical standards. CRA Trainees are typically involved in site visits, data verification, documentation, and communication between study sites and sponsors. Their role serves as a foundation for advancing to more senior CRA positions within the clinical research field.
Clinical Research Associate Trainee jobs near you
Infographic showing various Clinical Research Associate Trainee job openings in Raleigh, NC as of August 2026, with employment types broken down into 3% As Needed, 71% Full Time, 18% Part Time, and 8% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $63,772 per year, or $30.7 per hour.

Sr Clinical Research Associate

Veranex

Raleigh, NC • On-site

$98K - $140K/yr

Other

Posted 27 days ago

Job description

Veranex's mission as an Innovation CRO is to improve patient outcomes by accelerating our clients' innovations to market. As the world's only end-to-end professional services firm focused on MedTech, we take clients' Vision to Velocity through our comprehensive service portfolio, with expertise in human centered design and product development, preclinical and clinical research, regulatory affairs, and market access and reimbursement consulting.
The Veranex Clinical Operations team is a dynamic group of professionals providing regulatory, quality and clinical services for the medical device industry. Our team supports start-ups, mid-sized private companies, and the largest corporations at all stages of the product life cycle. We work across a broad spectrum of technologies and treatment modalities. Our clients develop both next-generation and paradigm-shifting devices. Our product exposure includes implantables, instruments (manual, laser, robotic, etc.), capital equipment, combination products, software as a medical device (SaMD), medical mobile apps, in vitro diagnostics and more
About This Role:
Veranex has an exciting opportunity to join our team as a Senior Clinical Research Associate to support our Clinical Operations team. The Sr. CRA will participate in the planning, development, and execution of clinical trials to evaluate the safety, effectiveness and performance of medical devices. Under management supervision, the Sr. CRA will monitor assigned clinical trials to ensure adherence to the clinical protocol, applicable regulations, and company Standard Operating Procedures (SOPs) governing clinical studies.
Location: Remote, US
What You Will Do:
  • Responsible for ensuring that study investigators and coordinators comply with the study protocol, Good Clinical Practices (GCPs), Code of Federal Regulations (CFRs), and Institutional Review Board (IRB)/Ethics Committee (EC) requirements during clinical studies by training/guidance of investigators/research coordinators, conducting periodic on-site evaluations and follow-up of corrective actions
  • Acts as primary liaison to clinical sites.
  • Conducts site qualification visits, study start-up activities (essential document collection), site qualification visits, site initiation visits and training, monitoring visits for source data verification (reported study data are accurate, complete, and verifiable from source documents in the site's medical records), and site close-out visits. Generates high-quality site qualification, initiation, monitoring, and close-out visit reports in timely manner (in accordance with the Clinical Monitoring Plan)
  • Contributes to protocol, informed consent, case report form (CRF) and study plan development as well as annual progress reports (APRs) and the clinical study report (CSR) at study conclusion to report the study results to FDA and other regulatory authorities
  • Ensures that the rights and well-being of human subjects are protected and confirms data quality/integrity by maintaining site compliance, reviewing adverse events and device deficiencies, reviewing data trending/metrics, reviewing audit reports, and implementing corrective actions as necessary
  • Supports maintenance of department SOPs and work instructions
  • Supports investigational device traceability including documentation for forecasting, shipping, receipt, and disposition.
  • Supports and maintains documentation of all clinical research activities in the study trial master file (TMF), e.g., monitoring reports, site correspondence, device inventory information.
  • Drives trial enrollment and identifies and communications potential and actual obstacles to enrollment.
  • Travel requirement: 25-50%

Qualifications:
Required skills:
  • Minimum of 5 years of directly related work experience or equivalent in clinical research, including work on medical device significant risk IDE trials and/or non-significant risk abbreviated IDE trials.
  • Must be able to work autonomously and as a member of a cross-functional team and meet high expectations and tight deadlines. May work on highly visible projects in high-pressure situations
  • Must have working knowledge of Good Clinical Practices (GCPs), FDA regulations and IRB requirements.
  • Must have strong project management competencies and ability to work with high quality, reliability, and attention to detail.
  • Must have a strong level of professionalism, including verbal and written communication skills; and the ability to communicate with all levels of the organization, cross-functionally, and with clients/partners.
  • Must have proficiency in using Microsoft Office Suite, including Word, Excel, Outlook and PowerPoint; as well as experience with electronic data capture (EDC) and electronic Trial Master File (eTMF) systems.
  • Experience interfacing successfully with physicians/clinical staff and familiarity with hospital/clinical environments
  • Familiarity with medical and anatomical terminology.
  • Ability and willingness to travel

Preferred:
  • BS or BA degree preferred; BS or BA in a relevant scientific discipline or related field also preferred.

Veranex is an equal opportunity employer and prohibits discrimination of any kind. All qualified applicants will receive consideration for employment without regard for race, color, religion or belief, sex (including pregnancy, gender identity or gender expression), sexual orientation, parental or marital status, disability, age, status as a protected veteran, national, social, or ethnic origin, or any other applicable legally protected characteristics.

Apply